Down-Regulation of MiR-127 Facilitates Hepatocyte Proliferation during Rat Liver Regeneration

被引:58
作者
Pan, Chuanyong [1 ]
Chen, Huan [1 ]
Wang, Lianghua [1 ]
Yang, Shengsheng [1 ]
Fu, Hailong [2 ]
Zheng, Yongxia [1 ]
Miao, Mingyong [1 ]
Jiao, Binghua [1 ]
机构
[1] Second Mil Med Univ, Dept Biochem & Mol Biol, Shanghai, Peoples R China
[2] Second Mil Med Univ, Changzheng Hosp, Dept Anaesthesiol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
CENTER B-CELLS; PARTIAL-HEPATECTOMY; GENE-EXPRESSION; HISTONE METHYLTRANSFERASE; MICRORNA EXPRESSION; S-PHASE; P53; METHYLATION; BCL6; MICE;
D O I
10.1371/journal.pone.0039151
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Liver regeneration (LR) after partial hepatectomy (PH) involves the proliferation and apoptosis of hepatocytes, and microRNAs have been shown to post-transcriptionally regulate genes involved in the regulation of these processes. To explore the role of miR-127 during LR, the expression patterns of miR-127 and its related proteins were investigated. MiR-127 was introduced into a rat liver cell line to examine its effects on the potential target genes Bcl6 and Setd8, and functional studies were undertaken. We discovered that miR-127 was down-regulated and inversely correlated with the expression of Bcl6 and Setd8 at 24 hours after PH, a time at which hypermethylation of the promoter region of the miR-127 gene was detected. Furthermore, in BRL-3A rat liver cells, we observed that overexpression of miR-127 significantly suppressed cell growth and directly inhibited the expression of Bcl6 and Setd8. The results suggest that down-regulation of miR-127 may be due to the rapid methylation of its promoter during the first 24 h after PH, and this event facilitates hepatocyte proliferation by releasing Bcl6 and Setd8. These findings support a miRNA-mediated negative regulation pattern in LR and implicate an anti-proliferative role for miR-127 in liver cells.
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页数:10
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